Ch1: Basic Pharm Flashcards

1
Q

Dose-Response Curves (DRC)

A

Range of drug doses - should go from undetectable effect to a dose so high that increases in dose have no further effect, and a number of doses in between

X axis: dose
Y axis: effect

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2
Q

ED50

A

Median effective dose - the dose that is effective in 50% of the individuals tested

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3
Q

LD50

A

Median lethal dose - the dose that kills 50% of those tested

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4
Q

Therapeutic Index/Ratio (TI)

A

Describes the safety of a drug

TI = LD50/ED50

Drug safety can also be described as a ratio of ED99 and LD1

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5
Q

Potency

A

Differences in the ED50 of two drugs. Drug with lower ED50 is more potent.

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6
Q

Effectiveness/efficacy

A

Differences in the maximum effect that the drugs will produce at any dose

Eg. aspirin and morphine are both painkillers, but aspirin at its most effective dose is not as effective as morphine

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7
Q

Antagonism

A

Drug interactions - one drug diminishes the effect of another drug

DRC is shifted to the right (i.e., ED50 increases) by adding new drug

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8
Q

Additive Effect

A

Effects of the combination = the sum of the expected effects of the two drugs alone

DRC is shifted to the left (i.e., ED50 decreases) by adding new drug

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9
Q

Superadditive Effect/ Potentiation

A

Effects of the combination is greater than the expected sum of the two drugs

Eg. if one drug has no effect alone but increases the effect of a second drug

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10
Q

Three processes of pharmacokinetics

A

1) Absorption: how a drug gets into blood
2) Distribution: where it goes into the body
3) Elimination: how the drug leaves the body

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11
Q

Routes of administration

A

1) Parenteral
2) Inhalation
3) Oral administration
4) Transdermal administration

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12
Q

Parenteral routes of administration

A
  • Vehicle: dissolve drug in liquid (called vehicle) before it’s injected
  • Subcutaneous: injected to form a bolus under the skin or tissue
  • Intramuscular: injected into a muscle
  • Intraperitoneal: injected into peritoneal cavity
  • Intravaneous: injected into a vein, directly into bloodstream
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13
Q

Absorption from parenteral sites

A

Fasted from ip injection, slowest from sc injection. Drug must pass through walls of capillaries.

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14
Q

Inhalation routes of administrration

A
  • Gases: breathed into the lungs

- Smoke & solids

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15
Q

Distribution of drugs

A
  • Lipid solubility: drug is slowly released from the fat into the blood over a long period of time
  • Ion trapping: ionized molecules are not lipid soluble, so pKa of a drug can hasten or slow down its absorption
  • Blood-brain barrier
  • Active & passive transport across membranes
  • Protein binding
  • Placental barrier
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16
Q

Elimination of drugs

A
  • Metabolism
  • Liver & kidneys
  • First-pass metabolism: pass through liver before going anywhere else
17
Q

Factors that alter drug metabolism

A
  • Stimulation of enzyme systems
  • Depression of enzyme systems
  • Age
18
Q

Therapeutic Window

A

Level of the drug maintained in the blood - the range between being too high of a level (eg. unwanted side effects, no increase in therapeutic effect) & falling below a certain level (eg. no therapeutic effect)